{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72787",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution and the country of Canada",
      "recall_number": "Z-0606-2016",
      "product_description": "Baxter INTERLINK System, Y-Type Solution Set, 78 (2.0 m), 2 Injection Sites, Male Luer Lock Adapter, 1C8581 s,    Product Usage:  C8581: For the administration of fluids from a container into the patient\u0019s vascular system through a vascular access device.  .",
      "product_quantity": "9600 units",
      "reason_for_recall": "Potential for dark loose particulate matter (400 microns or smaller) on the spike of the spike adapter or solution set.",
      "recall_initiation_date": "20151130",
      "center_classification_date": "20160106",
      "termination_date": "20161030",
      "report_date": "20160113",
      "code_info": "Lot Numbers:  GR324012, GR325322, GR326769, and GF328518"
    }
  ]
}